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Individual lesions of <jats:styled-content style=\"fixed-case\">DCPG<\/jats:styled-content> share clinical and histologic similarities with infantile hemangioma (<jats:styled-content style=\"fixed-case\">IH<\/jats:styled-content>); endothelial glucose transporter 1 (<jats:styled-content style=\"fixed-case\">GLUT<\/jats:styled-content>\u20101), which is highly expressed in <jats:styled-content style=\"fixed-case\">IH<\/jats:styled-content> but generally not in pyogenic granulomas (<jats:styled-content style=\"fixed-case\">PG<\/jats:styled-content>), is an important diagnostic tool. Treatment for <jats:styled-content style=\"fixed-case\">DCPG<\/jats:styled-content> remains difficult. We describe a case of <jats:styled-content style=\"fixed-case\">DCPG<\/jats:styled-content> effectively treated with propranolol.<\/jats:p>","DOI":"10.1111\/pde.13689","type":"journal-article","created":{"date-parts":[[2018,10,15]],"date-time":"2018-10-15T08:13:48Z","timestamp":1539591228000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":6,"title":["Multifocal congenital pyogenic granuloma successfully treated with oral propranolol"],"prefix":"10.1111","volume":"36","author":[{"given":"Mana","family":"Alharbi","sequence":"first","affiliation":[{"name":"Dermatology Department Imam Muhammad ibn Saud I. 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